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  4. NDC Product Code: 33992-6156 Assured Pain Relief Hot Menthol

NDC 33992-6156 Assured Pain Relief Hot Menthol

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 33992-6156?
  4. Assured Pain Relief Hot Menthol Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
33992-6156
Proprietary Name:
Assured Pain Relief Hot Menthol
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Greenbrier International, Inc
Labeler Code:
33992
Product Label ID:
4588d98b-c905-4729-9b40-722c344284b9
FDA Application Number: [6]
part348
Marketing Category: [8]
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date: [9]
10-17-2014
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 33992-6156?

The NDC code 33992-6156 is assigned by the FDA to the product Assured Pain Relief Hot Menthol which is product labeled by Greenbrier International, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 33992-6156-3 2 pouch in 1 carton / 30 mg in 1 pouch. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Assured Pain Relief Hot Menthol?

DirectionsAdults and children 12 years of age and older: apply to affected area no more than 3 to 4 times daily.Children under 12 years of age: do not use, consult a doctor.For easy application: partially peel back protective film and apply exposed film and apply exposed patch to site of pain.Carefully remove remaining film while pressing patch to skin for secure adhesion.

Which are Assured Pain Relief Hot Menthol UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Assured Pain Relief Hot Menthol Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".